The rs1991517 polymorphism is a genetic risk factor for congenital hypothyroidism
Author:
Funder
DST-SERB
Publisher
Springer Science and Business Media LLC
Subject
Agricultural and Biological Sciences (miscellaneous),Environmental Science (miscellaneous),Biotechnology
Link
https://link.springer.com/content/pdf/10.1007/s13205-020-02273-7.pdf
Reference40 articles.
1. Agrawal P, Philip R, Saran S, Gutch M, Razi MS, Agroiya P, Gupta K (2015) Congenital hypothyroidism. Indian J Endocrinol Metab 19:221–227. https://doi.org/10.4103/2230-8210.131748
2. Alves EA, Cruz CM, Pimentel CP, Ribeiro RC, Santos AK, Caldato MC, Santana-da-silva LC (2010) High frequency of D727E polymorphisms in exon 10 of the TSHR gene in Brazilian patients with congenital hypothyroidism. J Pediatr Endocrinol Metab 23:1321–1328. https://doi.org/10.1515/jpem.2010.206
3. Balmiki N, Bankura B, Guria S, Das TK, Pattanayak AK, Sinha A, Chakrabarti S, Chowdhury S, Das M (2014) Genetic analysis of thyroid peroxidase (TPO) gene in patients whose hypothyroidism was found in adulthood in West Bengal, India. Endocr J 61:289–296. https://doi.org/10.1507/endocrj.ej13-0237
4. Ban Y, Greenberg DA, Concepcion ES, Tomer Y (2002) A germline single nucleotide polymorphism at the intracellular domain of the human thyrotropin receptor does not have a major effect on the development of Graves' disease. Thyroid 12:1079–1083. https://doi.org/10.1089/105072502321085171
5. Bayram B, Sonmez R, Bozari S, Onlu H, Turkoglu Z, Mutlu FS (2013) The association between development and progression of multinodular goiter and thyroid-stimulating hormone receptor gene D727E and P52T polymorphisms. Genet Test Mol Biomarkers 17:109–114. https://doi.org/10.1089/gtmb.2012.0263
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